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Sarah A Graham

Showing results (41-50 of 48) with videos related to

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Human Molecular Genetics|January 25, 2018
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disordersSara B Estruch, Sarah A Graham, Martí Quevedo, et al.
Nature Communications|September 19, 2014
De novo TBR1 mutations in sporadic autism disrupt protein functionsPelagia Deriziotis, Brian J O'Roak, Sarah A Graham, et al.
Human Molecular Genetics|June 28, 2018
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disordersSara B Estruch, Sarah A Graham, Martí Quevedo, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|February 11, 2021
Artificial Intelligence for Mental Health Care: Clinical Applications, Barriers, Facilitators, and Artificial WisdomEllen E Lee, John Torous, Munmun De Choudhury, et al.
Glycobiology|May 13, 2009
Targeted glycoproteomic identification of cancer cell glycosylationAlex S Powlesland, Paul G Hitchen, Simon Parry, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
American Journal of Human Genetics|July 26, 2016
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates TranscriptionCristina Dias, Sara B Estruch, Sarah A Graham, et al.
Plos Genetics|March 28, 2017
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignanciesRocio Acuna-Hidalgo, Pelagia Deriziotis, Marloes Steehouwer, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Human Molecular Genetics|January 25, 2018
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disordersSara B Estruch, Sarah A Graham, Martí Quevedo, et al.
Nature Communications|September 19, 2014
De novo TBR1 mutations in sporadic autism disrupt protein functionsPelagia Deriziotis, Brian J O'Roak, Sarah A Graham, et al.
Human Molecular Genetics|June 28, 2018
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disordersSara B Estruch, Sarah A Graham, Martí Quevedo, et al.
Biological Psychiatry. Cognitive Neuroscience and Neuroimaging|February 11, 2021
Artificial Intelligence for Mental Health Care: Clinical Applications, Barriers, Facilitators, and Artificial WisdomEllen E Lee, John Torous, Munmun De Choudhury, et al.
Glycobiology|May 13, 2009
Targeted glycoproteomic identification of cancer cell glycosylationAlex S Powlesland, Paul G Hitchen, Simon Parry, et al.
Human Molecular Genetics|December 10, 2015
Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderElliot Sollis, Sarah A Graham, Arianna Vino, et al.
American Journal of Human Genetics|July 26, 2016
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates TranscriptionCristina Dias, Sara B Estruch, Sarah A Graham, et al.
Plos Genetics|March 28, 2017
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignanciesRocio Acuna-Hidalgo, Pelagia Deriziotis, Marloes Steehouwer, et al.
Pageof 5